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The Hippocratic facies (Latin: facies Hippocratica) [1] is the change produced in the face recognisable as a medical sign known as facies and prognostic of death. It may also be seen as due to long illness , excessive defecation , or excessive hunger , when it can be differentiated from the sign of impending death.
As there is no known cure, life expectancy of people with progeria is 15 years, as of 2024. [59] At least 90 percent of patients die from complications of atherosclerosis, such as heart attack or stroke. [60] Mental development is not adversely affected; in fact, intelligence tends to be average to above average. [61]
Roberts syndrome, or sometimes called pseudothalidomide syndrome, is an extremely rare autosomal recessive genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, and legs.
Life expectancy may be shortened by respiratory complications arising from weakness of the muscles that aid breathing and swallowing. It was first described in four patients by Vucic and colleagues [ 3 ] working at the Massachusetts General Hospital in the United States ; subsequent reports from the United Kingdom, [ 4 ] Europe and Asia [ 5 ...
Cockayne syndrome is a rare but destructive disease usually resulting in death within the first or second decade of life. The mutation of specific genes in Cockayne syndrome is known, but the widespread effects and its relationship with DNA repair is yet to be well understood. [6]
Sometimes there is flushing on the affected side of the face due to dilation of blood vessels under the skin. The pupil's light reflex is maintained as this is controlled via the parasympathetic nervous system. [citation needed] In children, Horner's syndrome sometimes leads to heterochromia, a difference in eye color between the two eyes. [3]
Bottom line: While the triangle of death has a terrifying moniker and some very real theoretical science behind it, avoiding serious infections is totally doable by adhering to a single rule: Don ...
Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy. These calcium deposits decrease the size of cranial foramina, and can decrease the circumference of the cervical spinal canal ...